[Influence of mutations of proteinase-activated receptors F2R/PAR1 and F2RL1/PAR2 on inflammatory bowel disease]

Med Clin (Barc). 2008 Nov 8;131(16):609-11. doi: 10.1157/13127918.
[Article in Spanish]

Abstract

Background and objective: Inflammatory bowel disease (IBD) is a polygenic complex trait. The expression and presence in biopsiae from IBD patients points to a putative role of these genes in genetic susceptibility to IBD. This is the first association study on these genes in relation with IBD.

Patients and method: Two polymorphisms were analyzed within F2R/PAR1 and another one mapping to F2RL1/PAR2 in 778 healthy controls and 943 IBD cases (Crohn's disease and ulcerative colitis patients from 2 cohorts from Madrid and Granada).

Results: No significant differences in the distribution of the PARs' polymorphisms were found.

Conclusions: There is no evidence of association of the analyzed polymorphisms with IBD risk.

Publication types

  • English Abstract

MeSH terms

  • Cohort Studies
  • Colitis, Ulcerative / epidemiology
  • Colitis, Ulcerative / genetics*
  • Crohn Disease / epidemiology
  • Crohn Disease / genetics*
  • Exons / genetics
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Haplotypes / genetics
  • Humans
  • Introns / genetics
  • Linkage Disequilibrium
  • Mutagenesis, Insertional
  • Mutation*
  • Polymorphism, Single Nucleotide
  • Receptor, PAR-1 / genetics*
  • Receptors, Thrombin / genetics*
  • Risk
  • Spain / epidemiology

Substances

  • Receptor, PAR-1
  • Receptors, Thrombin
  • protease-activated receptor 3